ENST00000397196.7:c.328+405T>C
MANE Select
|
ENSP00000380379.2:n.328+405T>C
|
|
ENST00000310594.7:c.328+405T>C
|
ENSP00000308887.3:n.328+405T>C
|
|
ENST00000397196.6:c.328+405T>C
|
ENSP00000380379.2:n.328+405T>C
|
|
ENST00000537031.5:c.328+405T>C
|
ENSP00000439312.1:n.328+405T>C
|
|
ENST00000539198.5:c.328+405T>C
|
ENSP00000438414.1:n.328+405T>C
|
|
ENST00000542408.1:c.328+405T>C
|
ENSP00000440600.1:n.328+405T>C
|
|
ENST00000543071.5:c.328+405T>C
|
ENSP00000442348.1:n.328+405T>C
|
|
ENST00000545811.5:c.328+405T>C
|
ENSP00000445395.1:n.328+405T>C
|
|
NM_030775.2:c.328+405T>C
|
NP_110402.2:n.328+405T>C
|
|
NM_032642.2:c.328+405T>C
|
NP_116031.1:n.328+405T>C
|
|
XM_011521026.1:c.328+405T>C
|
XP_011519328.1:n.328+405T>C
|
|
XM_024449203.1:c.484+405T>C
|
XP_024304971.1:n.484+405T>C
|
|
XM_024449204.1:c.391+405T>C
|
XP_024304972.1:n.391+405T>C
|
|
XM_024449205.1:c.328+405T>C
|
XP_024304973.1:n.328+405T>C
|
|
XM_024449206.1:c.328+405T>C
|
XP_024304974.1:n.328+405T>C
|
|
XM_024449207.1:c.328+405T>C
|
XP_024304975.1:n.328+405T>C
|
|
XM_024449208.1:c.328+405T>C
|
XP_024304976.1:n.328+405T>C
|
|
XM_024449209.1:c.328+405T>C
|
XP_024304977.1:n.328+405T>C
|
|
NM_032642.3:c.328+405T>C
MANE Select
|
NP_116031.1:n.328+405T>C
|
|